Sentinel Diagnostics - FDA Registration 24e70ae337d55c3bdd39beec2b2c1047
Access comprehensive regulatory information for Sentinel Diagnostics in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 24e70ae337d55c3bdd39beec2b2c1047 and manufactured by Sentinel CH. S.p.A. The device was registered on October 06, 2022.
This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.
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FDA Official Data
24e70ae337d55c3bdd39beec2b2c1047
Sentinel Diagnostics
FDA ID: 24e70ae337d55c3bdd39beec2b2c1047
Device Classification
Brand Name
Sentinel Diagnostics
Registration Information
Analysis ID
24e70ae337d55c3bdd39beec2b2c1047
Registration Date
October 06, 2022
Manufacturer
Authorized Representative

